Basic information Safety Supplier Related

Labeled d8 Desmethyl Clozapine Hydrochloride

Basic information Safety Supplier Related

Labeled d8 Desmethyl Clozapine Hydrochloride Basic information

Product Name:
Labeled d8 Desmethyl Clozapine Hydrochloride
Synonyms:
  • Labeled d8 Desmethyl Clozapine Hydrochloride
  • N-DESMETHYLCLOZAPINE (D8, 98%) 100 UG/ML IN METHANOL
  • [2H8]-N-Desmethyl Clozapine
  • 6-chloro-10-[(2,2,3,3,5,5,6,6-2H?)piperazin-1-yl]-2,9-diazatricyclo[9.4.0.03,?]pentadeca-1(11),3(8),4,6,9,12,14-heptaene
  • N-Desmethylclozapine-D8 solution
  • D8-N-Desmethyl Clozapine
CAS:
1189888-77-4
MF:
C17H17ClN4
MW:
312.8
Mol File:
1189888-77-4.mol
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Labeled d8 Desmethyl Clozapine Hydrochloride Chemical Properties

storage temp. 
Store at -20°C
solubility 
DMF: 10 mg/ml,DMSO: 10 mg/ml,DMSO:PBS (pH 7.2) (1:1): 0.5 mg/ml,Ethanol: 5 mg/ml
form 
A solid
color 
White to off-white
Major Application
clinical testing
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Safety Information

WGK Germany 
WGK 2
Storage Class
3 - Flammable liquids
Hazard Classifications
Acute Tox. 3 Dermal
Acute Tox. 3 Inhalation
Acute Tox. 3 Oral
Flam. Liq. 2
STOT SE 1
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Labeled d8 Desmethyl Clozapine Hydrochloride Usage And Synthesis

Uses

A major labelled metabolite of clozapine. A potent and selective 5-HT2C serotonin receptor antogonist.

Biological Activity

N-Desmethylclozapine-d8 is intended for use as an internal standard for the quantification of N-desmethylclozapine by GC- or LC-MS. N-Desmethylclozapine is an active metabolite of the atypical antipsychotic clozapine .1 It was originally described as an antagonist of serotonin (5-HT) receptor subtype 5-HT2C (IC50 = 7.1 nM in rat choroid plexus) and later as an inverse agonist using human recombinant receptors.2,3 N-Desmethylclozapine is an antagonist at dopamine D4 receptors, an agonist at δ-opioid receptors, and a partial agonist at dopamine D2 and D3, M1 muscarinic acetylcholine, and 5-HT1A receptors.3,1,4 N-Desmethylclozapine (30 mg/kg) decreases exploratory locomotor activity and increases prepulse inhibiton of the acoustic startle response in mice.5

IC 50

mAChR1; δ Opioid Receptor/DOR

References

1.Burstein, E.S., Ma, J., Wong, S., et al.Intrinsic efficacy of antipsychotics at human D2, D3, and D4 dopamine receptors: Identification of the clozapine metabolite N-desmethylclozapine as a D2/D3 partial agonistJ. Pharmacol. Exp. Ther.315(3)1278-1287(2005) 2.Kuoppam?ki, M., Syv?lahti, E., and Hietala, J.Clozapine and N-desmethylclozapine are potent 5-HT1C receptor antagonistsEur. J. Pharmacol.245(2)179-182(1993) 3.Lameh, J., Burstein, E.S., Taylor, E., et al.Pharmacology of N-desmethylclozapinePharmacol. Ther.115(2)223-231(2007) 4.Odagaki, Y., Kinoshita, M., and Ota, T.Comparative analysis of pharmacological properties of xanomeline and N-desmethylclozapine in rat brain membranesJ. Psychopharmacol.30(9)896-912(2016) 5.Maehara, S., Hikichi, H., and Ohta, H.Behavioral effects of N-desmethylclozapine on locomotor activity and sensorimotor gating function in mice-Possible involvement of muscarinic receptorsBrain Res.1418111-119(2011)

Labeled d8 Desmethyl Clozapine HydrochlorideSupplier

Artis Biotech Co. Ltd.
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19138486554; 18108108965
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sales@artisbio.com
Shanghai EFE Biological Technology Co., Ltd.
Tel
021-65675885 18964387627
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info@efebio.com
Shanghai YuanYe Biotechnology Co., Ltd.
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021-61312847; 18021002903
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3008007409@qq.com
Chengdu Novel Biomedical Co., Ltd.
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028-85255396 18302801538
Email
cdnovell@163.com
Energy Chemical
Tel
021-58432009 400-005-6266
Email
marketing1@energy-chemical.com
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